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Methyl benzene to benzoic acid
hot, alkaline, KMnO4, reflux, (dilute)
alcohol to haloalkane
kcl, conc h2so4 or H3po4
carboxylic acid to acyl chloride
pcl3, heat or pcl5
SO2 reaction w NaOH
Na2SO3 + H2O
ketone to hyrdroxynitrile
HCN, KCN heat
PCl5 + H2O
H3PO4, HCl
P4O10 + H2O
H3PO4
Phenylamine to phenol
heat, water (N2 gas) (black oily product)
Phenylamine to diazonium ion
HNO2, Ice, 5, HCl
Formation of nitrous acid (unstable)
NaNO2, HCl, Ice
Formation of Azo dye (diazonium ion is electrophile)
Diazonium ion, Phenol, NaOH (deprotonate)
Benzene to cyclohexane
H2, Pt (or Ni heat)
Phenol to trinitrophenol
Conc HNO3
Benzene to Nitrobenzene
Conc, H2SO4, HNO3, reflux, 55
Nitrile to amine
H2, Ni or LiAlH4, dry ether
Amine to Amide
Acyl chloride, cold
Amide to Amine
LiAlH4, dry ether
compare amide hydrolysis with acid vs alkali
COOH, ammonium salt vs COO- ion, NH3
Nitrile to carboxylic acid
dilute HCl, H2O, reflux
Compare nitrile hydrolysis w acid vs alkali
COOH, ammonium salt vs COO- ion, NH3
ester to COOH or OH (acid)
dilute H2SO4, reflux
ester to COOH or OH (alkali)
NaOH, HCl, reflux
relative acidities of carboxylic acids (1), phenols (2) and alcohols (3) (least to most)
321
Relative acidities: ethanoic acid (1), chloroethanoic acid (2) least to most
12
Phenylamine to tribromophenylamine
Br2, (room temp) (white ppt)
Acyl chloride + NH3
Amide
Acyl chloride + Amine
Amide
COOH + SOCl2
Acyl chloride, SO2, H2O
COOH + PCl5
Acyl chloride, POCl3, HCl
Methanoic acid to CO2, H2O
Hot, conc, acidified, KMnO4
Acyl Chloride to COOH
H2O
COOH + PCl3
heat, acyl chloride, H3PO3
Alcohol to Alkene (w/o catalyst)
conc, H2SO4, 180, reflux
Alcohol to Alkene (w catalyst)
Hot, Al2O3
Alcohol to chloroalkane
KCl, conc H2SO4
by product organic + PCl3
H3PO3
by product organic + PCl5
POCl3
by product organic + SOCl2
SO2
Haloalkane to nitrile
KCN, reflux, alcoholic
Haloalkane to amine
XS NH3 (or amine), Pressure, Alcoholic,
Alkene to Alkane
H2, Ni, 150
Alkene to Alcohol
Steam, H3PO4, 60 atm, 300
thermal cracking conditions
1200k, 7000Kpa
catalytic cracking condtions
zeolite, 720k
nitrobenzene to phenylamine
Sn, conc, hcl, reflux
amide + reducing agent
amine
diazonium ion to phenol
heat (>10) h2o